OSS Modular Arthrodesis Nail — Class II medical device recall Z-1036-2023
Ongoing recall by Biomet, Inc., reported 2023-02-08, distributed nationwide. Product missing the four small locking collar bolts resulting in extension of surgery to find a replacement
| Recall number | Z-1036-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2022-11-29 |
| Classified | 2023-01-27 |
| Reported by FDA | 2023-02-08 |
| Distributed | Nationwide (US) |
| Quantity | 2 units |
| UPC / GTIN / UDI-DI | 00880304082991 |
| Lot numbers | 136620 |
| Model numbers | CP260602 |
Product
OSS Modular Arthrodesis Nail, 7 Degree Collar Assembly with Locking Bolts-For use in the replacement of segmental defects of long bone, including midshaft replacement, and arthrodesis of the knee Item Number: CP260602
Reason for recall
Product missing the four small locking collar bolts resulting in extension of surgery to find a replacement
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1036-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.